Abstract
Fetal alcohol exposure (FAE) produces profound alterations in immunological and neuroendocrine functions. The present study examined the effects of FAE on the secretion of tumor necrosis factor (TNF-α) and corticosterone following administration of lipopolysaccharide (LPS) in normal (N) adult rats, in adult offspring of dams fed a liquid diet supplemented with ethanol (E), and in pair-fed control offspring (P). LPS-induced TNF-α secretion was not affected by either gender or prenatal treatment. In contrast, LPS-induced corticosterone secretion was significantly greater in female than in male rats, and at 60-min post-LPS was significantly higher in E and P, compared to N females. Ovariectomy significantly inhibited LPS- induced TNF-α secretion in E, but not in P and N, rats and chronic replacement with 17-β-estradiol markedly inherited TNF-α secretion in ovariectomized E and N, but not in P, rats. In contrast, ovariectomy reduced the effects of LPS on corticosterone secretion in all groups, and chronic replacement with 17-β-estradiol reversed this effect. These findings indicate that LPS-induced secretion of corticosterone, but not TNF-α, is affected by prenatal manipulations and by gender. In addition, alterations in the hormonal environment in females modulate LPS-induced corticosterone secretion in all prenatal treatment groups, but differentially influence TNF- α secretion in rats exposed to alcohol, restricted feeding, or normal diets in utero.
Original language | English |
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Pages (from-to) | 327-335 |
Number of pages | 9 |
Journal | Alcohol |
Volume | 15 |
Issue number | 4 |
DOIs | |
State | Published - May 1998 |
Bibliographical note
Funding Information:We thank Dr. Michelle L. Pilati and Mr. Ngy S. Heng for their assistance and contribution to this study. This research was supported by grants from the NIH/NIAAA (AA09850) and the Department of Veterans Affairs Medical Research Service (A. N. T.), and by grant No. 94-62 from the United States–Israel Binational Science Foundation (R. Y. and A. N. T.).
Keywords
- Corticosterone
- Estrogen
- Fetal alcohol exposure
- Lipopolysaccharide (LPS)
- Ovariectomy
- Prenatal food restriction
- Tumor necrosis factor-α